Canonical Allele Identifier: CA2710936263
Gene: ELOVL2 HGNC NCBI

Linked Data

dbSNP Id: rs2113453336

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10982133C>G , CM000668.2:g.10982133C>G GRCh38
NC_000006.11:g.10982366C>G , CM000668.1:g.10982366C>G GRCh37
NC_000006.10:g.11090352C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000354666.4:c.*1648G>C MANE Select ENSP00000346693.3:n.*1648G>C
ENST00000354666.3:c.*1648G>C ENSP00000346693.3:n.*1648G>C
NM_017770.3:c.*1648G>C NP_060240.3:n.*1648G>C
XM_011514716.1:c.*1648G>C XP_011513018.1:n.*1648G>C
XM_011514717.1:c.*1648G>C XP_011513019.1:n.*1648G>C
XM_011514716.3:c.*1648G>C XP_011513018.1:n.*1648G>C
NM_017770.4:c.*1648G>C MANE Select NP_060240.3:n.*1648G>C